Publication:
Lack of association between toll-like receptor 2 polymorphisms and susceptibility to severe disease caused by Staphylococcus aureus

dc.contributor.authorCatrin E. Mooreen_US
dc.contributor.authorShelley Segalen_US
dc.contributor.authorAnthony R. Berendten_US
dc.contributor.authorAdrian V.S. Hillen_US
dc.contributor.authorNicholas P.J. Dayen_US
dc.contributor.otherJohn Radcliffe Hospitalen_US
dc.contributor.otherNuffield Orthopaedic Centre NHS Trusten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Oxforden_US
dc.date.accessioned2018-07-24T03:36:23Z
dc.date.available2018-07-24T03:36:23Z
dc.date.issued2004-11-01en_US
dc.description.abstractTo investigate a putative link between genetically determined variations in Toll-like receptor 2 (TLR2) and the occurrence of severe Staphylococcus aureus infection, the functional Arg753Gln single-nucleotide polymorphism and the GT repeat microsatellite in the TLR2 gene were examined in a large case-control study. No associations with disease or mortality attributable to these features were found.en_US
dc.identifier.citationClinical and Diagnostic Laboratory Immunology. Vol.11, No.6 (2004), 1194-1197en_US
dc.identifier.doi10.1128/CDLI.11.6.1194-1197.2004en_US
dc.identifier.issn1071412Xen_US
dc.identifier.other2-s2.0-9144264994en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/21140
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=9144264994&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleLack of association between toll-like receptor 2 polymorphisms and susceptibility to severe disease caused by Staphylococcus aureusen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=9144264994&origin=inwarden_US

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